G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Reported: March 29, 2023 Initiated: February 6, 2023 #Z-1284-2023
Product Description
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
Reason for Recall
The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
Details
- Recalling Firm
- Biomet, Inc.
- Units Affected
- 12 units
- Distribution
- US Distribution to states of: AZ, FL, GA, MI, NE, and TX.
- Location
- Warsaw, IN
Frequently Asked Questions
What product was recalled? ▼
G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462. Recalled by Biomet, Inc.. Units affected: 12 units.
Why was this product recalled? ▼
The outer package labeling and product etch are a 40 mm Size D liner, however, the implant is a 38 mm Size C liner.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 29, 2023. Severity: Moderate. Recall number: Z-1284-2023.
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